| Literature DB >> 31350684 |
Shoh Sasaki1,2, Ran Tomomasa3, Sumihito Nobusawa3, Junko Hirato3,4, Tomoko Uchiyama5, Eishu Boku6, Toshiteru Miyasaka7, Takanori Hirose8, Chiho Ohbayashi5.
Abstract
Here, we report a rare case of anaplastic pleomorphic xanthoastrocytoma (PXA) associated with an H3G34 mutation. A 12-year-old male presented with loss of appetite, vomiting, headache, and a generalized seizure, and CT revealed a 9.0 cm left frontal lobe mass with some septal walls and a localized high-density area suggestive of hemorrhage or calcification, causing severe midline shift. He emergently underwent subtotal resection and the tumor was morphologically diagnosed as anaplastic PXA. DNA sequencing identified an H3F3A G34R mutation and a TP53 R273H mutation, and immunohistochemically, ATRX nuclear expression was lost. In CNS tumors, H3G34 mutations are essentially detected in glioblastoma (GBM) or central nervous system primitive neuroectodermal tumors. Those tumors most likely comprise a single biological entity (high-grade glioma with H3G34 mutation) because of no significant difference in molecular profiling and prognosis between GBM and PNET morphologies. To our knowledge, our present case is the first one of anaplastic PXA associated with an H3G34 mutation, and whether it biologically corresponds to "high-grade glioma with H3G34 mutation" needs further studies.Entities:
Keywords: ATRX; Anaplastic pleomorphic xanthoastrocytoma; H3G34 mutation; Olig2; TP53
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Year: 2019 PMID: 31350684 DOI: 10.1007/s10014-019-00349-8
Source DB: PubMed Journal: Brain Tumor Pathol ISSN: 1433-7398 Impact factor: 3.298